Validation Engineer
Job ID:  007-034 # Positions:  1
Location:  US- Experience (Years):  2
Posted Date:  3/18/2009 Category:  Validation Engineer - All Openings

More information about this job:
 
Overview:

Join our growing and progressive team! ProPharma Group, a Kansas City based company, serves the validation, compliance and technical service needs of clients in the pharmaceutical, biotechnology and medical device industries. Our validation professionals include chemical, electrical, mechanical and computer engineers, chemists, microbiologists and other specialists. ProPharma Group provides an excellent work environment and a culture of experience, integrity, and commitment. We offer a competitive salary and benefits package including: up to 12 paid holidays, paid vacation and sick time, health and dental insurance, 401K plan, employer paid short and long term disability, flexible spending plan, and life insurance. We are seeking Validation Engineers in the San Francisco, St. Louis, Kansas City and Kalamazoo, Michigan areas.



Responsibilities:
  • Performs all functions of a Validation Engineer.
  • Working knowledge of Validation and the principles of Validation as associated with performance of work for the Pharmaceutical, Biotechnology and/or Medical Device industries.
  • Reading basic engineering drawings including, but not limited to: P&ID's, Process and Utility Flow Diagrams, HVAC diagrams, Equipment and Instrumentation drawings.
  • Areas of experience include: process validation, computer validation, utilities validation, facilities validation and control systems validation, QA and solid dosage.


Qualifications:
  • Demonstrates an understanding of GMP.
  • Experience with temperature mapping, biologics, packaging and HVAC/Facilities.
  • Ability to execute protocols including complex systems such as process validation, computer controlled systems validation, complex utilities and manufacturing equipment such as computer controlled filling systems, formulation systems and basis knowledge of laboratory validation.
  • Understanding of the basic GMP skills and FDA cGMP's, FDA Guidelines and European guidelines (where applicable).
  • Working knowledge of Microsoft Word, Microsoft Excel.
  • Must have strong attention to detail.
  • Must have strong technical writing skills.
  • Effective written and oral communication skills; ability to write, type, express or exchange ideas of a technical nature.
  • Ability to travel up to 100%.

Education Requirements:

  • BS/BA in Engineering or Science or related field as a minimum.

 



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